Authors: Gerber, S Perrault, I Hanein, S Barbet, F Ducroq, D Ghazi, I Martin-Coignard, D Leowski, C Homfray, T Dufier, JL Munnich, A Kaplan, J Rozet, JM

Citation: S. Gerber et al., Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis, EUR J HUM G, 9(8), 2001, pp. 561-571